Canonical Allele Identifier: CA2269950065

Gene: ACE

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63497326G= , CM000679.2:g.63497326G=	GRCh38
NC_000017.10:g.61574687G= , CM000679.1:g.61574687G=	GRCh37
NC_000017.9:g.58928419G=	NCBI36
NG_011648.1:g.25254G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290866.10:c.3881G= MANE Select	ENSP00000290866.4:p.Gly1294=
ENST00000290863.10:c.2159G=	ENSP00000290863.6:p.Gly720=
ENST00000290866.9:c.3881G=	ENSP00000290866.4:p.Gly1294=
ENST00000413513.7:c.2036G=	ENSP00000392247.3:p.Gly679=
ENST00000428043.5:c.*303G=	ENSP00000397593.2:n.*303G=
ENST00000577647.2:c.1969+341G=	ENSP00000464149.1:n.1969+341G=
ENST00000578839.5:c.*1636G=	ENSP00000462110.2:n.*1636G=
ENST00000579314.5:c.*1610G=	ENSP00000462599.1:n.*1610G=
NM_000789.3:c.3881G=	NP_000780.1:p.Gly1294=
NM_001178057.1:c.2036G=	NP_001171528.1:p.Gly679=
NM_152830.2:c.2159G=	NP_690043.1:p.Gly720=
XM_005257110.1:c.3332G=	XP_005257167.1:p.Gly1111=
XM_006721737.2:c.2219G=	XP_006721800.2:p.Gly740=
XM_006721737.3:c.2219G=	XP_006721800.2:p.Gly740=
NM_000789.4:c.3881G= MANE Select	NP_000780.1:p.Gly1294=
NM_001178057.2:c.2036G=	NP_001171528.1:p.Gly679=
NM_152830.3:c.2159G=	NP_690043.1:p.Gly720=
NM_001382700.1:c.3314G=	NP_001369629.1:p.Gly1105=
NM_001382701.1:c.3029G=	NP_001369630.1:p.Gly1010=
NM_001382702.1:c.1496G=	NP_001369631.1:p.Gly499=
NR_168483.1:n.2259G=